(Q34980069)

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Tetrasomy 15q25.3 --> qter resulting from an analphoid supernumerary marker chromosome in a patient with multiple anomalies and bilateral Wilms tumors

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Europe PubMed Central

PubMed publication ID

5 August 2017

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Europe PubMed Central

Tetrasomy 15q25.3 --> qter resulting from an analphoid supernumerary marker chromosome in a patient with multiple anomalies and bilateral Wilms tumors (English)

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

1 reference

based on heuristic

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author name string

Hu J

1

1 reference

Europe PubMed Central

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5 August 2017

McPherson E

2

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Europe PubMed Central

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5 August 2017

Surti U

3

1 reference

Europe PubMed Central

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5 August 2017

Hasegawa SL

4

1 reference

Europe PubMed Central

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5 August 2017

Gunawardena S

5

1 reference

Europe PubMed Central

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5 August 2017

Gollin SM

6

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5 August 2017

language of work or name

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1 November 2002

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5 August 2017

American Journal of Medical Genetics Part A

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5 August 2017

113

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Europe PubMed Central

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5 August 2017

1

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Europe PubMed Central

PubMed publication ID

5 August 2017

82-88

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PubMed publication ID

5 August 2017

Forty four probands with an additional "marker" chromosome.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10708

21 January 2018

Plasma insulin-like growth factor-I and prostate cancer risk: a prospective study

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10708

21 January 2018

Centromere DNA dynamics: latent centromeres and neocentromere formation

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10708

21 January 2018

Characterization of neo-centromeres in marker chromosomes lacking detectable alpha-satellite DNA.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10708

21 January 2018

Perlman and Wiedemann-Beckwith syndromes: two distinct conditions associated with Wilms' tumour

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10708

21 January 2018

Comparative genomic hybridization analysis of hepatoblastomas

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10708

21 January 2018

Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10708

21 January 2018

An infant with deletion of the distal long arm of chromosome 15 (q26.1----qter) and loss of insulin-like growth factor 1 receptor gene.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10708

21 January 2018

Relaxation of insulin-like growth factor 2 imprinting and discordant methylation at KvDMR1 in two first cousins affected by Beckwith-Wiedemann and Klippel-Trenaunay-Weber syndromes

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10708

21 January 2018

Mosaic tetrasomy 15q25-->qter in a newborn infant with multiple anomalies.

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10708

21 January 2018

Increased expression of the insulin-like growth factor I receptor gene, IGF1R, in Wilms tumor is correlated with modulation of IGF1R promoter activity by the WT1 Wilms tumor gene product

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10708

21 January 2018

Mutation in fibrillin-1 and the Marfanoid-craniosynostosis (Shprintzen-Goldberg) syndrome

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10708

21 January 2018

Chromosomal sublocalization of human c-myb and c-fes cellular onc genes

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10708

21 January 2018

Abnormal Stat activation, hematopoietic homeostasis, and innate immunity in c-fes-/- mice

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10708

21 January 2018

Identifiers

10.1002/AJMG.10708

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

5 August 2017

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